Ontology highlight
ABSTRACT: Background
Age-related macular degeneration (AMD), the most common cause of blindness in the developed world, usually affects individuals older than 60 years of age. The majority of visual loss in this disease is attributable to the development of choroidal neovascularization (CNV). Mononuclear phagocytes, including monocytes and their tissue descendants, macrophages, have long been implicated in the pathogenesis of neovascular AMD (nvAMD). Current therapies for nvAMD are based on targeting vascular endothelial growth factor (VEGF). This study is aimed at assessing if perturbation of chemokine signaling and mononuclear cell recruitment may serve as novel complementary therapeutic targets for nvAMD.Methods
A promiscuous chemokine antagonist (BKT130), aflibercept treatment, o
SUBMITTER: Hagbi-Levi S
PROVIDER: S-EPMC6701410 | biostudies-literature | 2019
REPOSITORIES: biostudies-literature